Gene · 5428
Papers4,408
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
201 to 220 of 4,408
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Genetic profiling of azoospermic men to identify the etiology and predict reproductive potential. | J Assist Reprod Genet | 2024 | 38403804 | PubTator, text mining | PubMed |
| The NAD+ Precursor Nicotinamide Riboside Rescues Mitochondrial Defects and Neuronal Loss in iPSC derived Cortical Organoid of Alpers' Disease. | Int J Biol Sci | 2024 | 38385069 | PubTator, text mining | PubMed |
| Teaching Video NeuroImage: TWNK Mutation Causes Chronic Progressive External Ophthalmoplegia and Cerebellar Ataxia: A POLG-Like Phenotype. | Neurology | 2024 | 38315955 | PubTator, text mining | PubMed |
| Oligogenic basis of premature ovarian insufficiency: an observational study. | J Ovarian Res | 2024 | 38310280 | PubTator, text mining | PubMed |
| Cancer Precision-Prevention trial of Metformin in adults with Li Fraumeni syndrome (MILI) undergoing yearly MRI surveillance: a randomised controlled trial protocol. | Trials | 2024 | 38308321 | PubTator, text mining | PubMed |
| Optic Neuropathy Associated with POLG Mutations: A Case Series and Literature Review. | J Neuroophthalmol | 2024 | 38294884 | PubTator, text mining | PubMed |
| Advances in crosstalk among innate immune pathways activated by mitochondrial DNA. | Heliyon | 2024 | 38268572 | PubTator, text mining | PubMed |
| Genetic Testing of Movements Disorders: A Review of Clinical Utility. | Tremor Other Hyperkinet Mov (N Y) | 2024 | 38222898 | PubTator, text mining | PubMed |
| Clinical and genetic profile of patients with dystonia: An experience from a tertiary neurology center from India. | Parkinsonism Relat Disord | 2024 | 38219528 | PubTator, text mining | PubMed |
| Relationship between Biochemical Pathways and Non-Coding RNAs Involved in the Progression of Diabetic Retinopathy. | J Clin Med | 2024 | 38202299 | PubTator, text mining | PubMed |
| Analysis of rare Parkinson's disease variants in millions of people. | NPJ Parkinsons Dis | 2024 | 38191580 | PubTator, text mining | PubMed |
| Reverse vaccinology and immunoinformatics approach to design a chimeric epitope vaccine against Orientia tsutsugamushi. | Heliyon | 2024 | 38187223 | PubTator, text mining | PubMed |
| Protein biomarkers GDF15 and FGF21 to differentiate mitochondrial hepatopathies from other pediatric liver diseases. | Hepatol Commun | 2024 | 38180987 | PubTator, text mining | PubMed |
| The mitochondrial DNA common deletion as a potential biomarker of cancer-associated fibroblasts from skin basal and squamous cell carcinomas. | Sci Rep | 2024 | 38177205 | PubTator, text mining | PubMed |
| Biallelic pathogenic variants of PARS2 cause developmental and epileptic encephalopathy with spike-and-wave activation in sleep. | Mol Genet Genomic Med | 2024 | 38087948 | PubTator, text mining | PubMed |
| POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotype. | Clin Neurol Neurosurg | 2024 | 38070461 | PubTator, text mining | PubMed |
| Endocrine features of primary mitochondrial diseases. | Curr Opin Endocrinol Diabetes Obes | 2024 | 38047549 | PubTator, text mining | PubMed |
| The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions. | Mol Genet Genomic Med | 2024 | 38018320 | PubTator, text mining | PubMed |
| Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations. | Pediatr Transplant | 2024 | 38012111 | PubTator, text mining | PubMed |
| Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes. | Clin Neurol Neurosurg | 2024 | 37455189 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
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GET https://conductscience.org/api/genes/v1/5428/papers?page=11